HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Fluoride → Ethyl 3-(3thienyl)phenoxyacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Ethyl 2-(3-bromophenoxy)acetate | HCID 5197439 | — |
| Reactant | Stannane, tributyl-3-thienyl- | HCID 10959689 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Ethyl 3-(3thienyl)phenoxyacetate | HCID 19916940 | 64.6% |
Reaction Steps
2.6 g of the resulting ether compound, 5.3 g of tri-n-butyl(3-thienyl)tin and 20 mg of tetrakis(triphenylphosphine)palladium were dissolved in 10 ml of xylene, and the mixture was refluxed for 5.5 hours. A 25% aqueous solution of potassium fluoride was added to the solution, and then the precipitate was removed by filtration. The organic layer separated was worked up in a customary manner, and the product was purified by silica gel column chromatography [hexane/ethyl acetate=20/1→15/1] to give 1.7 g of ethyl 3-(3thienyl)phenoxyacetate as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05439932 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-f7b35241cf3940bdb8f07315907b7130 |
| Source note | uspto-grants-1995_08 |